GE Healthcare Recalls
567 recalls on record · June 27, 2012 to April 8, 2026 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare 1.5T SIGNA HDe MR System, nuclear magnetic resona
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE 0.7T SIGNA OpenSpeed with Excite MR System, nuclear magnetic
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA OpenSpeed MR System, nuclear magnetic reson
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA HFO/I MR System, nuclear magnetic resonance
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Infinity MR System, SIGNA Infinity MR Syste
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA 1.5T TwinSpeed MR System, nuclear magnetic
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE 1.5T SIGNA HDx MR System, GE 3.0T SIGNA HDx MR System, GE 1.
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR450 1.5T system, nuclear magnetic res
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare Optima MR450w 1.5T, Optima MR450w GEM system, nuc
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Artist system, nuclear magnetic resonance i
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Voyager and SIGNA Voyager Premier Edition s
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA MR380 System, nuclear magnetic resonance sy
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA MR355 and SIGNA MR360 System, nuclear magne
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Creator and SIGNA Explorer System, nuclear
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA PET/MR System, tomographic imager combining
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750 3.0T System, nuclear magnetic res
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare Discovery MR750w 3.0T System, nuclear magnetic re
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Pioneer System, nuclear magnetic resonance
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Architect system, nuclear magnetic resonanc
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 16, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Premier System, nuclear magnetic resonance
Hazard: The magnetic resonance systems could potentially have a cryogen ventilation system that does not meet the venting requirements.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector Wi-Fi"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector USB"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Sector DICOM"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Dual Wi-Fi"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Dual USB"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Dual DICOM"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
February 2, 2022Medical DevicesFDA
GE Healthcare, LLC recalls GE Vscan Extend, being sold as "Vscan Extend Console"
Hazard: The firm identified that the Vscan Extend device will not power on because of depleted battery, due to the device not being turned off prior to battery removal or when being connected to a computer without AC power.
December 8, 2021Medical DevicesFDA
GE Healthcare, LLC recalls GE Centricity Universal Viewer Zero Footprint Client
Hazard: There is a potential to display incomplete patient imaging study.
December 1, 2021Medical DevicesFDA
GE Healthcare, LLC recalls Computed Tomography Systems Revolution CT, Revolution CT ES, Revolution Apex, Revolution CT with Apex edition
Hazard: The accumulated dose is incorrectly displayed in certain situations. Thisoccurs during an interventional exam using the SmartStep option if the table height is adjusted after the exam starts. In this situation, the SmartStep display will show a value that is higher (up to 100 times) than the actual dose delivered.
October 27, 2021Medical DevicesFDA
GE Healthcare, LLC recalls 1.5T SIGNA HDxt MR System nuclear magnetic resonance imaging system
Hazard: Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.